Hydrochloric Acid → HCID 14800369, compound

HRID 1073717Notes

Reaction equation

HRID 1073717 reaction equation
C([O:4][C:5]1[CH:6]=[C:7]([CH:39]=[CH:40][C:41]=1[O:42]C(=O)C)[CH2:8][N:9]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=2[C:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[N:12][CH:11]([NH:26][C:27]([C:29]2[NH:30][C:31]3[C:36]([CH:37]=2)=[CH:35][CH:34]=[CH:33][CH:32]=3)=[O:28])[C:10]1=[O:38])(=O)C.CO.C(=O)([O-])[O-].[K+].[K+].Cl>O.C(OCC)(=O)C.O1CCCC1>[OH:4][C:5]1[CH:6]=[C:7]([CH:39]=[CH:40][C:41]=1[OH:42])[CH2:8][N:9]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=2[C:13]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[N:12][CH:11]([NH:26][C:27]([C:29]2[NH:30][C:31]3[C:36]([CH:37]=2)=[CH:35][CH:34]=[CH:33][CH:32]=3)=[O:28])[C:10]1=[O:38]

Participants

8

Procedure

A mixture of (3RS)-1-(3,4-diacetoxybenzyl)-1,3-dihydro-3-(2-indolylcarbonylamino) -5-phenyl-2H-1,4-benzodiazepine-2-one (287 mg), methanol (5 ml), tetrahydrofuran (5 ml), water (1 ml) and 1N aqueous potassium carbonate (5 ml) was stirred for 1.0 hour at 0 - 5° C. and then adjusted to pH 1-2 with 6N hydrochloric acid. Ethyl acetate (50 ml) and water (50 ml) were added to the mixture under stirring. The separated organic layer was washed with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel with an eluent of a mixture of chloroform and ethyl acetate (4:1) to give (3RS)-1(3,4-dihydroxybenzyl) -3-(2-indolylcarbonylamino)-5-phenyl-2H-1,4-benzodiazepine-2-one (155 mg).

Workup

  1. stirringunder stirring
  2. washThe separated organic layer was washed with water
  3. dry with materialdried over magnesium sulfate
  4. customevaporated
  5. customThe residue was chromatographed on silica gel with an eluent of a mixture of chloroform and ethyl acetate (4:1)

Sources & evidence

ORD record
ord-e783560a1f60475684d5693a1eb97513
Source dataset
uspto-grants-1990_11
Patent number
US04970207

Reaction notes

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